Type I spinal muscular atrophy and disease modifying treatments: a nationwide study in children born since 2016Research in context
Summary: Background: The advent of disease-modifying treatments (DMT) has changed natural history in 5q Spinal muscular atrophy (SMA). The aim of this study was to report survival and functional aspects in all the Italian type I children born since 2016. Methods: The study included all symptomatic...
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          | Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , | 
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| Format: | Article | 
| Language: | English | 
| Published: | Elsevier
    
        2024-12-01 | 
| Series: | EClinicalMedicine | 
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2589537024005467 | 
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